Friedreich's ataxia is an autosomal recessive disease caused by trinucleotide repeat expansion, presenting among other systemic complications, diabetes mellitus. The appearance of motor clumsiness, with running and jumping difficulties in a 6-year-old boy prompted the genetic study of Friedreich's ataxia, confirming his diagnosis. After diagnosis, it was evaluated by Pediatric Cardiology, detecting the presence of non-obstructive hypertrophic cardiomyopathy, and by Pediatric Endocrinology, due to overweight. At 9 years of age, he was diagnosed with diabetes mellitus, a regimen of insulin treatment was initiated. During follow-up, he presented significant neurological deterioration, reaching the use of a wheelchair, which hinders adequate metabolic control. This is a report of a pediatric patient with Friedrich ataxia and diabetes mellitus.
CITATION STYLE
Cabrero, A. M., Raspeño, M. E., Escudero, V. S., Cruz, N. G., & Vergaz, A. G. (2022). Diabetes mellitus and Friedreich’s ataxia in a child: A complicated coexistence. Archivos Argentinos de Pediatria, 120(5), E223–E225. https://doi.org/10.5546/aap.2022.e223
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